EP2721650A1 - Procede de realisation d'une cellule photovoltaique a emetteur selectif - Google Patents
Procede de realisation d'une cellule photovoltaique a emetteur selectifInfo
- Publication number
- EP2721650A1 EP2721650A1 EP12726462.0A EP12726462A EP2721650A1 EP 2721650 A1 EP2721650 A1 EP 2721650A1 EP 12726462 A EP12726462 A EP 12726462A EP 2721650 A1 EP2721650 A1 EP 2721650A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- photovoltaic cell
- producing
- type
- substrate
- antireflection layer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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Classifications
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
- H10F71/00—Manufacture or treatment of devices covered by this subclass
- H10F71/129—Passivating
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
- H10F10/00—Individual photovoltaic cells, e.g. solar cells
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
- H10F10/00—Individual photovoltaic cells, e.g. solar cells
- H10F10/10—Individual photovoltaic cells, e.g. solar cells having potential barriers
- H10F10/14—Photovoltaic cells having only PN homojunction potential barriers
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
- H10F71/00—Manufacture or treatment of devices covered by this subclass
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
- H10F71/00—Manufacture or treatment of devices covered by this subclass
- H10F71/121—The active layers comprising only Group IV materials
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
- H10F71/00—Manufacture or treatment of devices covered by this subclass
- H10F71/128—Annealing
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
- H10F77/00—Constructional details of devices covered by this subclass
- H10F77/30—Coatings
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
- H10F77/00—Constructional details of devices covered by this subclass
- H10F77/30—Coatings
- H10F77/306—Coatings for devices having potential barriers
- H10F77/311—Coatings for devices having potential barriers for photovoltaic cells
- H10F77/315—Coatings for devices having potential barriers for photovoltaic cells the coatings being antireflective or having enhancing optical properties
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10P—GENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
- H10P32/00—Diffusion of dopants within, into or out of wafers, substrates or parts of devices
- H10P32/10—Diffusion of dopants within, into or out of semiconductor bodies or layers
- H10P32/14—Diffusion of dopants within, into or out of semiconductor bodies or layers within a single semiconductor body or layer in a solid phase; between different semiconductor bodies or layers, both in a solid phase
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10P—GENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
- H10P32/00—Diffusion of dopants within, into or out of wafers, substrates or parts of devices
- H10P32/10—Diffusion of dopants within, into or out of semiconductor bodies or layers
- H10P32/14—Diffusion of dopants within, into or out of semiconductor bodies or layers within a single semiconductor body or layer in a solid phase; between different semiconductor bodies or layers, both in a solid phase
- H10P32/1408—Diffusion of dopants within, into or out of semiconductor bodies or layers within a single semiconductor body or layer in a solid phase; between different semiconductor bodies or layers, both in a solid phase from or through or into an external applied layer, e.g. photoresist or nitride layers
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10P—GENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
- H10P32/00—Diffusion of dopants within, into or out of wafers, substrates or parts of devices
- H10P32/10—Diffusion of dopants within, into or out of semiconductor bodies or layers
- H10P32/17—Diffusion of dopants within, into or out of semiconductor bodies or layers characterised by the semiconductor material
- H10P32/171—Diffusion of dopants within, into or out of semiconductor bodies or layers characterised by the semiconductor material being group IV material
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10P—GENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
- H10P34/00—Irradiation with electromagnetic or particle radiation of wafers, substrates or parts of devices
- H10P34/40—Irradiation with electromagnetic or particle radiation of wafers, substrates or parts of devices with high-energy radiation
- H10P34/42—Irradiation with electromagnetic or particle radiation of wafers, substrates or parts of devices with high-energy radiation with electromagnetic radiation, e.g. laser annealing
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/52—PV systems with concentrators
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/547—Monocrystalline silicon PV cells
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
Definitions
- the invention relates to a method for manufacturing a selective emitter photovoltaic cell comprising an n-doped or p-doped silicon substrate, as well as zones of low doping and high n doping.
- the field of use of the present invention is also directed to the production of electricity from solar energy and more particularly from photons.
- a photovoltaic cell The operation of a photovoltaic cell is mainly based on the absorption of photons generating the passage of electrons between the valence band and the conduction band of a material with semiconducting properties constituting the cell. .
- This electron transfer is made possible by doping the material constituting the photovoltaic cell, so as to create areas with an excess of electrons (n-doping) as well as areas with an electron defect (p-doping).
- a photovoltaic cell comprises a p-doped silicon substrate covered with an n-doped silicon layer.
- This stack constitutes a pn junction necessary for the collection of photo-carriers generated by the exposure of the photovoltaic cell to sunlight.
- the n-doped silicon layer is also covered with an antireflection layer ensuring good photon absorption. The latter comprises electrical contacts for collecting the generated current.
- the selective emitter cells have been developed. These cells have zones of high doping n as well as zones of low doping n in an n-type or p-type substrate.
- the selective emitter solar cells of the prior art therefore comprise a layer of low doping n, also called zone or region n + or n + emitter.
- the transmitter also includes areas of high doping n (n ++ regions or n ++ transmitters) precisely defined to make electrical contacts. The n + emitter thus makes it possible to facilitate passivation by the antireflection layer and to reduce Auger recombination while the n ++ emitter is connected to the electrical contacts in order to ensure good ohmic contact.
- the methods of manufacturing such a selective emitter photovoltaic cell according to the prior art comprise the following steps:
- an antireflection layer typically silicon nitride by PECVD (English acronym for "Plasma Enhanced Chemical Vapor Deposition") ( Figure 1D);
- a metallization gate (contact n) on the upper face of the substrate.
- This is typically a silkscreen silver paste.
- the patterns of this metallization gate are precisely aligned with the emitters n in order to avoid short-circuiting the n + emitter during annealing of the contacts (FIG. 1E). Indeed, if the metallization is shifted above the n-zone, the latter being thin, during annealing, the metal can pass through it and bring the n-zone into contact with the substrate. • Deposition of a paste containing aluminum (p-contact) on the entire underside of the substrate.
- BSF Back Surface Field
- FOG. 1E passivation by field effect
- the step of forming the n + emitter and that of annealing the contacts n and the contacts p are incompatible and can not be performed simultaneously.
- the step of forming the n + emitter by gaseous diffusion of a dopant (POCI3) is relatively long (several tens of minutes), and would lead to short-circuit the areas under the electrical contacts if it were performed. after depositing said contacts.
- a dopant POCI3
- pasta used in screen printing, method used to make electrical contacts are incompatible with the furnaces used for the diffusion of dopants, because they implement large amounts of metals that would irremediably pollute the diffusion furnaces.
- the methods of the prior art therefore comprise incompatible steps, each requiring a very specific energy supply.
- the present invention makes it possible to reduce these energy constraints by combining certain steps of the manufacture of a photovoltaic cell with a selective emitter.
- the Applicant has developed a method for manufacturing a selective emitter photovoltaic cell in which the n + emitter, the n contacts, the p contacts, and the BSF effect are made simultaneously during a single step of annealing.
- the invention makes it possible to remedy certain problems of the prior art related to the incompatibility of the annealing and diffusion stages of n dopants.
- the present invention relates to a method for manufacturing a selective emitter photovoltaic cell comprising the following steps:
- an antireflection layer comprising n-type dopants on a n-type or p-type silicon substrate, said deposition being carried out in the presence of a chemical compound making it possible to accelerate the diffusion of the n-type doping atoms in the silicon substrate n-type;
- the dopants n n ++ overdoped transmitters can also broadcast. As a result, the resulting contact is even deeper.
- point diffusion it is meant that only the dopants n of at least one precise zone of the antireflection layer are diffused so as to form n ++ regions constituting the n ++ emitters. Moreover, during the annealing step of the electrical contacts, and therefore of the formation of the n + emitter, this at least one zone of the antireflection layer whose dopants n have been diffused to form the n + zone or zones + , does not contribute to the formation of the transmitter n + .
- the type of silicon is defined by the metallurgy of the ingot of origin of the substrate used during the crystallization. Typically, p-type silicon is doped with boron and n-type silicon is doped with phosphorus.
- the antireflection layer is made of silicon nitride, advantageously by PECVD (Plasma Enhanced Chemical Vapor Deposition).
- PECVD Plasma Enhanced Chemical Vapor Deposition
- it is doped n, preferably with phosphorus, generally during the deposition, for example using a doping gas.
- the antireflection layer may possibly no longer be doped.
- the chemical compound that makes it possible to accelerate the diffusion of the n-type doping atoms is advantageously ammonia. Without emitting any theory, it is possible that the layer of silicon nitride obtained in the presence of ammonia, NH 3 , is less dense than the silicon nitride layers of the prior art, obtained in the presence of nitrogen, N 2 .
- the n dopants, phosphorus atoms can thus move more freely.
- the n ++ zones can be produced in particular by laser doping, advantageously by irradiation using a pulsed laser, and more advantageously still of a pulsed laser whose wavelength can be chosen in the field extending from ultraviolet to infrared.
- the laser has a wavelength substantially equal to 515 nm.
- the laser doping step may eventually lead to partial removal of the antireflection layer.
- n ++ zones make it possible to ensure a good contact at the level of the upper face of the substrate, while avoiding any short circuit.
- the n ++ zones are very deep and are performed prior to the step of making the electrical contacts by annealing the conductive materials n and p. They are at a depth advantageously greater than 0.5 micrometre relative to the upper face of the antireflection layer. They are advantageously deeper than the n + zones.
- the duration of the laser pulses is preferably between 10 ps and 1 ⁇ .
- the n and p type conductive materials are deposited by screen printing. This technique involves depositing a paste on the substrate previously covered with a mask. The dough is then pushed by a squeegee at an adjustable speed and pressure. The properties of the mask and in particular its thickness are defined according to the electrical contacts to be formed. In the case of n contacts, these pasta advantageously contain little glass frit to limit the risk of short circuit.
- the thickness of the substrate is between 50 micrometers and 500 micrometers while the antireflection layer has a thickness of between 20 and 100 nanometers.
- the n + emitter and the electrical contacts are simultaneously produced by annealing in an infrared oven.
- This step is preferably carried out at a temperature of between 850 and 1050 ° C., and at a speed of passage of the substrate in the furnace, advantageously between 2000 and 6500 mm / min.
- the passage time in the oven is advantageously between 1 s and 60 s. Consequently, it is particularly advantageous for the doping source to be stable in the air in order to be able to be diffused during the passage of the substrate in an oven.
- the presence of a chemical compound for accelerating the diffusion of the n-type dopant atoms is crucial. Indeed, this compound ensures greater mobility in the doping steps, and in particular during the production of the electrical contacts by annealing the n and p conducting materials, during which the n + emitter is formed by diffusion of the n doping atoms.
- the present invention also relates to a photovoltaic cell capable of being obtained according to the manufacturing method described above. This cell comprises a n-type or p-type silicon substrate containing at least:
- an antireflection layer positioned on the upper face of the substrate
- n + emitter on which is positioned a contact n physically independent of the antireflection layer and the n + emitter.
- the combination of the steps concerning the diffusion of the transmitter n and the making of the contacts by annealing is contrary to the teaching of the prior art, since they implement very distinct energy constraints. . Indeed, the formation of the n + emitter by diffusion is generally carried out in a vacuum oven at the temperature of 850 ° C. for 30 minutes, whereas the annealing of the electrical contacts is carried out in the open air and at temperatures from 800 to 900 ° C for 3 minutes only. Although the temperatures of these two processes remain similar, the respective annealing times vary in a ratio of 1/10.
- the energy input necessary for producing the electrical contacts n and p by annealing the conductive materials is very much lower than that required for the formation of the n + emitter by diffusion.
- This difference is mainly explained by the fact that the doping particles (and for example phosphorus) diffuse very slowly in the silicon, which requires very long durations to create a n + emitter sufficiently doped to ensure a good performance.
- metal particles providing electrical contacts especially silver or aluminum
- the realization of electrical contacts by annealing therefore requires a lower energy input and therefore a lower annealing time with respect to the diffusion of dopants n. It is also important to ensure that the annealing time remains short in order to prevent the metal particles from diffusing too deeply and completely through the n + emitter, which would lead to a very poor cell efficiency (short cell -circuottie).
- the metal contacts can not be deposited prior to the formation of the n + emitter by diffusion in a traditional diffusion tube (ie in quartz and under vacuum). Indeed, it would result in a pollution of the diffusion tube by releasing the metal particles contained in the contacts with respect to the high temperatures used and in particular the time required for the diffusion process.
- this combination is made possible by the presence of a chemical compound, advantageously ammonia, making it possible to accelerate the diffusion of the dopant atoms n under less energetic conditions.
- a n + emitter of good quality that is to say, to obtain Voc> 620 mV
- the Voc represents the open circuit voltage, it is an electrical characteristic of the diode.
- Those skilled in the art will also be able to adjust the durations of the different diffusion and annealing steps depending on the composition of the photovoltaic cell. Indeed, the duration of the annealing depends in particular on the temperature but also the dopant, and electrical contacts and vice versa.
- FIGS. 1A to 1F illustrate the steps of producing a selective emitter photovoltaic cell according to the prior art.
- FIG. 1F represents a photovoltaic cell with a selective emitter of the prior art.
- FIGS. 2A to 2E illustrate the steps of producing a selective emitter photovoltaic cell according to the present invention.
- FIG. 2E represents a photovoltaic cell with a selective emitter according to the invention. DETAILED DESCRIPTION OF THE FIGURES
- FIGS. 1A to 1F The steps of the method of manufacturing a selective emitter photovoltaic cell according to the prior art are described below in the light of FIGS. 1A to 1F. These figures more particularly represent sectional views of a photovoltaic cell according to the prior art during the different manufacturing steps.
- the substrate is of type p.
- FIG. 1A shows a p-type silicon substrate (1).
- an n + emitter (5) is produced by n-doping of the substrate (1). It may in particular be doping by gaseous diffusion in the presence of POCI 3 , in the case of n doping with phosphorus. This step therefore consists in maintaining the substrate at a temperature of 850 to 950 ° C. for several tens of minutes, the diffusion of the dopant being relatively slow.
- FIG. 1C illustrates the embodiment of an emitter n (6) by laser doping. This step can also be carried out by implementing a second gaseous diffusion of the dopant (POCI3). However, in this case the temperature would be higher than that at which the n + emitter (5) of Fig. 1C is made. Thus, some areas of the n + emitter are overdoped.
- POCI3 gaseous diffusion of the dopant
- FIG. 1D represents the deposition of an antireflection layer (2), typically silicon nitride by PECVD.
- the last step of the method according to the prior art concerns the production of electrical contacts (3) and (4) as illustrated by FIGS. 1E and 1F.
- a metallization grid is deposited on the upper face of the substrate so as to prepare the contacts n (3).
- This is typically a silkscreen silver paste.
- an aluminum-containing paste is deposited on the entire lower face of the substrate so as to prepare the contacts p (4).
- This paste makes it possible on the one hand to ensure contact with the p-doped part of the photovoltaic cell, and on the other hand to improve the electrical properties of the latter by BSF.
- the formation of the electrical contacts is finalized by simultaneous annealing of the pastes (silver and aluminum) in a passage oven, for example at a temperature of 885 ° C. and with a belt speed of 6500 mm / min in order to give the photovoltaic cell selective transmitter of the prior art as shown in Figure 1F.
- FIGS. 2A to 2E The various main steps of the method of manufacturing a selective emitter photovoltaic cell according to the present invention are described below in the light of FIGS. 2A to 2E. These figures more particularly represent the sectional views of a photovoltaic cell during the different manufacturing steps according to the invention.
- FIG. 2A represents a substrate (1) of p-type silicon, that is to say a substrate having an electron deficiency, and therefore an excess of holes considered to be positively charged.
- This substrate is generally obtained by doping a silicon substrate using atoms belonging to the previous column of the periodic table of the elements, such as boron.
- FIG. 2B illustrates the deposition of an n-doped antireflection layer (7) on the p-type silicon substrate (1).
- This antireflection layer (7) differs from the antireflection layer (2) of FIG. 1D (prior art) in that it comprises n-type dopants, that is to say atoms having an excess of electrons negatively. loaded. It may be a layer of silicon nitride doped with phosphorus atoms.
- the deposition of Si is generally carried out by PECVD using an NH 3 / S 1 H 4 mixture and in the presence of a PH 3 phosphine stream.
- Ammonia is used as a precursor gas, further enabling the mobility of the phosphorus atoms to be improved.
- the molar ratio NH 3 / S 1 H 4 is between 1 and 20.
- the p-doped silicon substrate is thus covered with an n-doped silicon nitride layer.
- the antireflection layer is doped n.
- Figure 2C shows the formation of n ++ (6) areas overdoped within the substrate.
- the n ++ (6) zones can be produced by laser irradiation, preferably by pulsed laser, the duration of the pulses being of the order of a few tens of nanoseconds.
- the wavelength of the laser can be chosen in the range extending from the ultraviolet (excimer laser at 308 nm for example) to the infrared (solid laser at 1064 nm for example). It is preferentially a laser whose wavelength is substantially equal to 515 nm.
- the n-doped antireflection layer (7) is irradiated locally, so as to create highly doped zones.
- the laser doping is associated with the partial ablation of the antireflection layer.
- this ablation is not essential within the meaning of the present invention.
- FIG. 2D represents the deposition of the conductive materials constituting the electrical contacts on the zones n (contacts n (3)) and on the zone p (contact (4)).
- the annotations (3) and (4) denote the conductive materials, that is to say the electrical contacts before annealing, and the electrical contacts made after annealing.
- the conductive material constituting the contacts n (3) typically silver, is deposited on the emitters n ++ (6).
- FIG. 2E illustrates contacts n (3) not being in contact with the antireflection layer (7), they can also be in contact with the antireflection layer (7) according to another embodiment of the invention. currently illustrated.
- the contacts p (4) are made of aluminum. The electrical contacts make it possible to collect the current generated subsequently by the photovoltaic cell.
- FIG. 2E concerns the embodiment of the n + emitter (5) by diffusion of the dopants of the n-doped silicon nitride antireflection layer (7) simultaneously with the production of the n (3) contacts and the p contacts. (4) annealing.
- This step consists of diffusing, in a single step at high temperature, the dopants contained in the SiN: P (7) antireflection layer in order to produce the n + emitter (5), while producing the electrical contacts by annealing the n contacts (3) and p (4) contacts, and the activation of the BSF.
- This step can be carried out in an infrared oven.
- a selective emitter photovoltaic cell is produced according to the following steps: 1.
- the surface of a p-type silicon substrate is chemically textured by dipping for 40 minutes in an aqueous solution, comprising 7% by volume of isopropanol, of potassium hydroxide (1% KOH) at 80 ° C.
- Areas of the antireflection layer are selectively irradiated to form, by laser doping, the n ++ emitter. This laser doping is performed by means of a pulsed laser having a wavelength of 515 nanometers.
- the duration of the pulses is 20 ns, with a rate of 300 kHz, corresponding to a power of 1.7 W.
- the diameter of the n ++ zones thus obtained is 40 micrometers for a laser shot. Larger areas can be obtained by repeating the laser shot by moving the point of impact.
- Electrical contacts are made by metallization by screen printing.
- the contact n in the form of juxtaposed lines consists of a silver paste (PV142 from Dupont), mask opening 70 micrometers, not openings of 2.1 millimeters, aligned on the n ++ zones.
- the contact p consists of an aluminum paste (PASE1202 from Monocrystal) deposited on the entire lower surface of the substrate. This contact constitutes a zone of high p doping to ensure the phenomenon of BSF.
- the diffusion formation of the n + emitter and the contacts n and the contacts p are carried out in a single step in a Centrotherm brand infrared oven, at a temperature of 1000 ° C., and a flow rate of 4000 mm / min. .
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- Photovoltaic Devices (AREA)
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Abstract
Description
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Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR1155352A FR2976727B1 (fr) | 2011-06-17 | 2011-06-17 | Procede de realisation d'une cellule photovoltaique a emetteur selectif |
| PCT/FR2012/050932 WO2012172226A1 (fr) | 2011-06-17 | 2012-04-26 | Procede de realisation d'une cellule photovoltaique a emetteur selectif |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP2721650A1 true EP2721650A1 (fr) | 2014-04-23 |
| EP2721650B1 EP2721650B1 (fr) | 2015-07-01 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP12726462.0A Active EP2721650B1 (fr) | 2011-06-17 | 2012-04-26 | Procédé de réalisation d'une cellule photovoltaïque a émetteur sélectif |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US8969186B2 (fr) |
| EP (1) | EP2721650B1 (fr) |
| JP (1) | JP6053764B2 (fr) |
| KR (1) | KR101892322B1 (fr) |
| CN (1) | CN103608934B (fr) |
| BR (1) | BR112013029066A2 (fr) |
| FR (1) | FR2976727B1 (fr) |
| WO (1) | WO2012172226A1 (fr) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103165758B (zh) * | 2013-04-01 | 2015-08-26 | 南通大学 | 一种基于逆扩散的太阳能电池选择性掺杂方法 |
| US20140315371A1 (en) * | 2013-04-17 | 2014-10-23 | International Business Machines Corporation | Methods of forming isolation regions for bulk finfet semiconductor devices |
| CN104143583B (zh) * | 2013-05-08 | 2016-08-03 | 昱晶能源科技股份有限公司 | 制造太阳能电池的方法及太阳能电池 |
| JP2016532317A (ja) * | 2013-09-27 | 2016-10-13 | ダンマークス テクニスク ユニバーシテットDanmarks Tekniske Universitet | ナノ構造化されたシリコン系太陽電池およびナノ構造化されたシリコン系太陽電池を製造する方法 |
| DE102014103303A1 (de) | 2014-03-12 | 2015-10-01 | Universität Konstanz | Verfahren zum Herstellen von Solarzellen mit simultan rückgeätzten dotierten Bereichen |
| USD951916S1 (en) * | 2020-11-19 | 2022-05-17 | Shenzhen Ginto E-commerce Co., Limited | Earphone |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS63283172A (ja) * | 1987-05-15 | 1988-11-21 | Sharp Corp | 太陽電池の製造方法 |
| JP3045917B2 (ja) * | 1994-01-28 | 2000-05-29 | シャープ株式会社 | 太陽電池の製造方法 |
| JP3368145B2 (ja) * | 1996-06-20 | 2003-01-20 | シャープ株式会社 | 太陽電池セルの製造方法 |
| AUPP437598A0 (en) * | 1998-06-29 | 1998-07-23 | Unisearch Limited | A self aligning method for forming a selective emitter and metallization in a solar cell |
| JP2007184251A (ja) * | 2005-12-07 | 2007-07-19 | Sony Corp | 表示装置 |
| KR20070099840A (ko) * | 2006-04-05 | 2007-10-10 | 삼성에스디아이 주식회사 | 태양 전지 및 이의 제조 방법 |
| KR101370126B1 (ko) * | 2008-02-25 | 2014-03-04 | 엘지전자 주식회사 | 탑햇 형태의 레이저 어닐링을 이용한 태양전지의 선택적에미터 형성방법 및 이를 이용한 태양전지의 제조방법 |
| US8053343B2 (en) * | 2009-02-05 | 2011-11-08 | Snt. Co., Ltd. | Method for forming selective emitter of solar cell and diffusion apparatus for forming the same |
| FR2943180A1 (fr) * | 2009-09-08 | 2010-09-17 | Commissariat Energie Atomique | Procede de formation d'une cellule photovoltaique avec dopage par laser |
| CN102054898B (zh) * | 2009-11-06 | 2012-10-31 | 国立清华大学 | 选择性射极太阳能电池的制程 |
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- 2012-04-26 JP JP2014515249A patent/JP6053764B2/ja not_active Expired - Fee Related
- 2012-04-26 EP EP12726462.0A patent/EP2721650B1/fr active Active
- 2012-04-26 CN CN201280025262.2A patent/CN103608934B/zh not_active Expired - Fee Related
- 2012-04-26 WO PCT/FR2012/050932 patent/WO2012172226A1/fr not_active Ceased
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- 2012-04-26 KR KR1020137031284A patent/KR101892322B1/ko not_active Expired - Fee Related
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Also Published As
| Publication number | Publication date |
|---|---|
| BR112013029066A2 (pt) | 2017-02-07 |
| KR20140027329A (ko) | 2014-03-06 |
| JP2014524140A (ja) | 2014-09-18 |
| FR2976727A1 (fr) | 2012-12-21 |
| CN103608934A (zh) | 2014-02-26 |
| FR2976727B1 (fr) | 2013-11-08 |
| EP2721650B1 (fr) | 2015-07-01 |
| WO2012172226A1 (fr) | 2012-12-20 |
| CN103608934B (zh) | 2016-01-27 |
| US20140087511A1 (en) | 2014-03-27 |
| US8969186B2 (en) | 2015-03-03 |
| KR101892322B1 (ko) | 2018-08-27 |
| JP6053764B2 (ja) | 2016-12-27 |
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